Variant report

Variant	nsv539903
Chromosome Location	chr9:587358-763007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2519)
CpG islands
(count:366)
Chromatin interactive
region (count:64)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:2519 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:755679-756377	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:745817-746038	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:706038-706477	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:744770-744894	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:734845-735045	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:726050-726236	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:710020-710338	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:716213-716255	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
18	BACH1	chr9:706737-707111	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr9:652937-653241	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr9:755733-756053	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
22	BATF	chr9:755709-756109	GM12878	blood:	n/a	chr9:755945-755954 chr9:755850-755861
23	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
26	BHLHE40	chr9:761513-761762	HepG2	liver:	n/a	n/a
27	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
28	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
29	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
30	BHLHE40	chr9:734758-735070	HepG2	liver:	n/a	n/a
31	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
34	BHLHE40	chr9:755691-756354	HepG2	liver:	n/a	n/a
35	BRCA1	chr9:756272-756352	HepG2	liver:	n/a	n/a
36	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:682572-683106	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:758246-758511	A549	lung:	n/a	chr9:758338-758349
39	CEBPB	chr9:758129-758534	MCF-7	breast:	n/a	chr9:758338-758349
40	CEBPB	chr9:693978-694256	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:694718-695117	A549	lung:	n/a	n/a
42	CEBPB	chr9:745772-746032	A549	lung:	n/a	chr9:745902-745913
43	CEBPB	chr9:599971-600359	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
44	CEBPB	chr9:673657-674592	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:756000-756376	K562	blood:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195
46	CEBPB	chr9:618414-618785	IMR90	lung:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
47	CEBPB	chr9:647176-647333	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr9:652997-653155	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr9:599936-600484	Hela-S3	cervix:	n/a	chr9:600087-600098 chr9:600123-600134
50	CEBPB	chr9:755785-756371	A549	lung:	n/a	chr9:756184-756197 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195 chr9:756186-756195

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:705143-705193	SK-N-MC	brain:	n/a
2	chr9:707166-707216	IMR90	lung:	fetal
3	chr9:707166-707216	NHBE	bronchial:	n/a
4	chr9:707387-707437	GM19239	blood:	n/a
5	chr9:705143-705193	MCF10A-Er-Src	breast:	n/a
6	chr9:707410-707460	LNCaP	prostate:	n/a
7	chr9:707166-707216	CMK	blood:	n/a
8	chr9:705143-705193	MCF-7	breast:	n/a
9	chr9:761482-761532	PFSK-1	brain:	n/a
10	chr9:714269-714319	GM19239	blood:	n/a
11	chr9:707166-707216	HMEC	breast:	n/a
12	chr9:707410-707460	HPAEpiC	pulmonary alveolar:	n/a
13	chr9:761482-761532	HRCEpiC	kidney:	n/a
14	chr9:761482-761532	HUVEC	blood vessel:	n/a
15	chr9:705143-705193	ovcar-3	ovarian:	n/a
16	chr9:714269-714319	NB4	blood:	n/a
17	chr9:761482-761532	GM12892	blood:	n/a
18	chr9:714269-714319	CMK	blood:	n/a
19	chr9:707387-707437	HRCEpiC	kidney:	n/a
20	chr9:707387-707437	MCF10A-Er-Src	breast:	n/a
21	chr9:714269-714319	Hepatocyte	liver:	n/a
22	chr9:707410-707460	Hela-S3	cervix:	n/a
23	chr9:705143-705193	ECC-1	luminal epithelium:	n/a
24	chr9:714269-714319	LNCaP	prostate:	n/a
25	chr9:707410-707460	SKMC	muscle:	n/a
26	chr9:707410-707460	AG09309	skin:	n/a
27	chr9:714269-714319	GM06990	blood:	n/a
28	chr9:707410-707460	Jurkat	blood:	n/a
29	chr9:714269-714319	MCF10A-Er-Src	breast:	n/a
30	chr9:761482-761532	MCF-7	breast:	n/a
31	chr9:761482-761532	IMR90	lung:	fetal
32	chr9:761482-761532	HCF	heart:	n/a
33	chr9:707410-707460	GM12891	blood:	n/a
34	chr9:705143-705193	PANC-1	pancreas:	n/a
35	chr9:705143-705193	AG04449	skin:	fetal
36	chr9:707166-707216	NH-A	brain:	n/a
37	chr9:714269-714319	K562	blood:	n/a
38	chr9:707387-707437	Caco-2	colon:	n/a
39	chr9:707410-707460	NB4	blood:	n/a
40	chr9:707387-707437	HEK293	kidney:	embryo
41	chr9:707387-707437	Jurkat	blood:	n/a
42	chr9:707410-707460	SK-N-SH	brain:	n/a
43	chr9:761482-761532	ECC-1	luminal epithelium:	n/a
44	chr9:714269-714319	SAEC	small airway:	n/a
45	chr9:707166-707216	NB4	blood:	n/a
46	chr9:761482-761532	AG10803	skin:	n/a
47	chr9:707387-707437	Hepatocyte	liver:	n/a
48	chr9:707166-707216	AG09319	gingival:	n/a
49	chr9:705143-705193	U87	brain:	n/a
50	chr9:707387-707437	RPTEC	kidney:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
2	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
3	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
4	chr9:385789..386423-chr9:612104..612846,2	K562	blood:
5	chr9:705245..708353-chr9:743847..747461,3	MCF-7	breast:
6	chr9:730043..732840-chr9:737557..739917,2	MCF-7	breast:
7	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
8	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
9	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
10	chr8:128752586..128753455-chr9:706903..707668,2	NB4	blood:
11	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
12	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
13	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
14	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
15	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
16	chr9:704209..707068-chr9:719899..721523,2	MCF-7	breast:
17	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
18	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
19	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
20	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
21	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
22	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
23	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
24	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
25	chr9:725965..727738-chr9:729421..731068,2	MCF-7	breast:
26	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
27	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
28	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
29	chr16:1239384..1239884-chr9:736833..737597,2	MCF-7	breast:
30	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
31	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
32	chr9:744945..746598-chr9:748652..750929,2	K562	blood:
33	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
34	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
35	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
36	chr9:734184..736441-chr9:739422..741192,2	MCF-7	breast:
37	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
38	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
39	chr9:706307..708254-chr9:737100..740465,4	MCF-7	breast:
40	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
41	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
42	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
43	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
44	chr9:697287..699295-chr9:705065..707332,2	K562	blood:
45	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
46	chr17:17584235..17586582-chr9:741151..743803,2	MCF-7	breast:
47	chr9:757453..760203-chr9:763946..765702,2	MCF-7	breast:
48	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
49	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
50	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-4	chr9:749336-749509	XLOC_007628
2	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
3	lnc-C9orf66-4	chr9:761299-761551	XLOC_007628
4	lnc-DMRT1-3	chr9:659986-660326	NONHSAT129934
5	lnc-C9orf66-4	chr9:749336-749496	XLOC_007628
6	lnc-KANK1-1	chr9:747272-747365	NONHSAT129937
7	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.3
8	lnc-C9orf66-5	chr9:755232-755507	XLOC_007629
9	lnc-KANK1-1	chr9:747412-747469	NONHSAT129937
10	lnc-KANK1-1	chr9:748000-751056	NONHSAT129937
11	lnc-C9orf66-5	chr9:752722-752856	XLOC_007629
12	lnc-C9orf66-4	chr9:747413-747469	XLOC_007628
13	lnc-C9orf66-3	chr9:677542-677628	ENSG00000227914.3
14	lnc-KANK1-1	chr9:746431-746497	NONHSAT129937
15	lnc-C9orf66-3	chr9:674124-674379	ENSG00000227914.3
16	lnc-C9orf66-3	chr9:673817-674379	ENSG00000227914.1
17	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.3
18	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.1
19	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.1
20	lnc-C9orf66-3	chr9:673478-674379	ENSG00000227914.3

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KANK1	hsa-miR-124-3p	chr9:746055-746062
2	KANK1	hsa-miR-10a-5p	chr9:745092-745115
3	KANK1	hsa-miR-124-3p	chr9:746043-746062
4	KANK1	hsa-miR-335-5p	chr9:746085-746104
5	KANK1	hsa-miR-335-5p	chr9:746049-746071

Variant related genes	Relation type
ENSG00000227914	TF binding region
KANK1	TF binding region
ENSG00000229875	TF binding region
ENSG00000227914	CpG island
KANK1	CpG island
ENSG00000229875	CpG island
ENSG00000107104	chromatin interactions
ENSG00000108557	chromatin interactions
ENSG00000227914	chromatin interactions
PPM1A	miRNA target sites
FAM123B	miRNA target sites
SOD2	miRNA target sites

Extended variants
information (count: 10699 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:10699 , 50 per page) page: 1 2 3 4 5 6 7 ... 214

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554670281	chr9:587374-587375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562186786	chr9:587403-587404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531193471	chr9:587406-587407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370515898	chr9:587463-587464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551216623	chr9:587489-587490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574724258	chr9:587497-587498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78134473	chr9:587508-587509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184327442	chr9:587511-587512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373912953	chr9:587519-587520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547532114	chr9:587521-587522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554126156	chr9:587564-587565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77065634	chr9:587655-587656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188700189	chr9:587662-587663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1494001	chr9:587663-587664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563069893	chr9:587677-587678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs137959793	chr9:587681-587682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116546462	chr9:587700-587701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1494000	chr9:587708-587709	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs566129946	chr9:587721-587722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534914761	chr9:587728-587729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117640065	chr9:587765-587766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574687155	chr9:587787-587788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561055880	chr9:587812-587813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550751710	chr9:587834-587835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529628054	chr9:587865-587866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143400344	chr9:587894-587895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575970523	chr9:587895-587896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546577758	chr9:587926-587927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566608460	chr9:588025-588026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112447268	chr9:588034-588035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564840125	chr9:588043-588044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200074474	chr9:588068-588069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77225847	chr9:588070-588071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112717290	chr9:588079-588080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147420100	chr9:588080-588081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74365571	chr9:588084-588085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540768130	chr9:588092-588093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561109561	chr9:588102-588103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529896471	chr9:588123-588124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181235585	chr9:588130-588131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569935624	chr9:588163-588164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562815060	chr9:588173-588174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200253042	chr9:588181-588182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552503843	chr9:588185-588186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80321579	chr9:588186-588187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7873324	chr9:588191-588192	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs186064457	chr9:588205-588206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371422131	chr9:588232-588233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572790565	chr9:588248-588249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72689652	chr9:588291-588292	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	21272361	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:6135 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:549800-593800	Weak transcription	Lung	lung
2	chr9:572000-589400	Weak transcription	Aorta	Aorta
3	chr9:572200-589800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr9:574400-589000	Weak transcription	Brain Substantia Nigra	brain
5	chr9:574600-589400	Weak transcription	HMEC	breast
6	chr9:575200-589200	Weak transcription	Right Ventricle	heart
7	chr9:575400-587400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr9:579800-589200	Weak transcription	Brain Anterior Caudate	brain
9	chr9:581400-588800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:581400-589600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr9:581400-591400	Weak transcription	Fetal Intestine Large	intestine
12	chr9:582000-589000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr9:582000-589400	Weak transcription	Esophagus	oesophagus
14	chr9:582000-591400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:582200-587600	Weak transcription	Fetal Intestine Small	intestine
16	chr9:582200-589200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr9:582200-589200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:582400-589000	Weak transcription	Right Atrium	heart
19	chr9:582400-589400	Weak transcription	A549	lung
20	chr9:582600-589200	Weak transcription	Pancreas	Pancrea
21	chr9:582600-591400	Weak transcription	Gastric	stomach
22	chr9:583000-588600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:583000-594400	Weak transcription	Fetal Kidney	kidney
24	chr9:584400-589600	Weak transcription	Stomach Mucosa	stomach
25	chr9:585200-589800	Enhancers	Fetal Heart	heart
26	chr9:585400-589200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr9:586800-589200	Weak transcription	Ovary	ovary
28	chr9:587000-588600	Weak transcription	Small Intestine	intestine
29	chr9:587000-589200	Weak transcription	Left Ventricle	heart
30	chr9:587200-587400	Enhancers	Brain Hippocampus Middle	brain
31	chr9:587200-588200	Weak transcription	Duodenum Mucosa	Duodenum
32	chr9:587400-587800	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr9:587400-588800	Weak transcription	Brain Hippocampus Middle	brain
34	chr9:587600-588000	Enhancers	Fetal Intestine Small	intestine
35	chr9:587800-589200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr9:588000-588200	Weak transcription	Fetal Intestine Small	intestine
37	chr9:588200-588800	Enhancers	Fetal Intestine Small	intestine
38	chr9:588200-590600	Enhancers	Duodenum Mucosa	Duodenum
39	chr9:588400-588600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr9:588400-588600	Enhancers	Rectal Smooth Muscle	rectum
41	chr9:588600-588800	Enhancers	Small Intestine	intestine
42	chr9:588600-589200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr9:588600-589200	Weak transcription	Rectal Smooth Muscle	rectum
44	chr9:588600-589600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr9:588800-589400	Weak transcription	Small Intestine	intestine
46	chr9:588800-589600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr9:588800-590200	Enhancers	Brain Hippocampus Middle	brain
48	chr9:588800-591000	Weak transcription	Fetal Intestine Small	intestine
49	chr9:588800-591400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:589000-589600	Enhancers	NHEK	skin

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